Interdent, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Interdent, Inc. makes
Interdent, Inc. manufactures dental dam products, including the FASTDAM system for isolating teeth during procedures, and a non-pressure autoclave designed for sterilizing dental instruments.
The company’s portfolio includes devices classified as Class I and Class II under FDA regulations, with products listed via the 510(k) pathway. These devices are registered in the United States.
Catalogue
Fastdam Ref K972775
Regimes: 510(k) Registry: 510(k)Non-Pressure Autoclave For Sterilization Ref K823457
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Interdent, Inc. have in the registry?
The registry currently lists 2 devices for Interdent, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Interdent, Inc.'s devices?
Among its 2 most recently registered devices, Interdent, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Interdent, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Interdent, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Interdent, Inc. in the registry?
The most recently registered devices listed for Interdent, Inc. include FASTDAM and NON-PRESSURE AUTOCLAVE FOR STERILIZATION.